Identification and Characterization of Splicing Defects by Single-Molecule Real-Time Sequencing Technology (PacBio).


Journal

Journal of neuromuscular diseases
ISSN: 2214-3602
Titre abrégé: J Neuromuscul Dis
Pays: Netherlands
ID NLM: 101649948

Informations de publication

Date de publication:
2020
Historique:
pubmed: 1 7 2020
medline: 23 7 2021
entrez: 30 6 2020
Statut: ppublish

Résumé

Although DNA-sequencing is the most effective procedure to achieve a molecular diagnosis in genetic diseases, complementary RNA analyses are often required.Reverse-Transcription polymerase chain reaction (RT-PCR) is still a valuable option when the clinical phenotype and/or available DNA-test results address the diagnosis toward a gene of interest or when the splicing effect of a single variant needs to be assessed.We use Single-Molecule Real-Time sequencing to detect and characterize splicing defects and single nucleotide variants in well-known disease genes (DMD, NF1, TTN). After proper optimization, the procedure could be used in the diagnostic setting, simplifying the workflow of cDNA analysis.

Identifiants

pubmed: 32597815
pii: JND200523
doi: 10.3233/JND-200523
doi:

Substances chimiques

Connectin 0
DMD protein, human 0
DNA, Complementary 0
Dystrophin 0
NF1 protein, human 0
Neurofibromin 1 0
TTN protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

477-481

Auteurs

Marco Savarese (M)

Folkhälsan Research Center, Helsinki, Finland.
Department of Medical Genetics, Medicum, University of Helsinki, Helsinki, Finland.

Talha Qureshi (T)

Folkhälsan Research Center, Helsinki, Finland.
Department of Medical Genetics, Medicum, University of Helsinki, Helsinki, Finland.

Annalaura Torella (A)

Dipartimento di Medicina di Precisione, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy.
Telethon Institute of Genetics and Medicine, Pozzuoli, Italy.

Pia Laine (P)

Institute of Biotechnology, University of Helsinki, Helsinki, Finland.

Teresa Giugliano (T)

Dipartimento di Medicina di Precisione, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy.

Per Harald Jonson (PH)

Folkhälsan Research Center, Helsinki, Finland.
Department of Medical Genetics, Medicum, University of Helsinki, Helsinki, Finland.

Mridul Johari (M)

Folkhälsan Research Center, Helsinki, Finland.
Department of Medical Genetics, Medicum, University of Helsinki, Helsinki, Finland.

Lars Paulin (L)

Institute of Biotechnology, University of Helsinki, Helsinki, Finland.

Giulio Piluso (G)

Dipartimento di Medicina di Precisione, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy.

Petri Auvinen (P)

Institute of Biotechnology, University of Helsinki, Helsinki, Finland.

Vincenzo Nigro (V)

Dipartimento di Medicina di Precisione, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy.
Telethon Institute of Genetics and Medicine, Pozzuoli, Italy.

Bjarne Udd (B)

Folkhälsan Research Center, Helsinki, Finland.
Department of Medical Genetics, Medicum, University of Helsinki, Helsinki, Finland.
Vaasa Central Hospital, Vaasa, Finland.

Peter Hackman (P)

Folkhälsan Research Center, Helsinki, Finland.
Department of Medical Genetics, Medicum, University of Helsinki, Helsinki, Finland.

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Classifications MeSH